UNCUFFED REINFORCED TRACHEAL TUBE
K-Number: K841872 · 1984-07-26
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Device Summary
Frequently Asked Questions
What is the UNCUFFED REINFORCED TRACHEAL TUBE?
UNCUFFED REINFORCED TRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1984-07-26. The listed applicant is Mallinckrodt Critical Care. The 510(k) number is K841872.
When did UNCUFFED REINFORCED TRACHEAL TUBE receive FDA 510(k) clearance?
UNCUFFED REINFORCED TRACHEAL TUBE received FDA 510(k) clearance on 1984-07-26, under 510(k) number K841872.
Who is the listed applicant for UNCUFFED REINFORCED TRACHEAL TUBE?
The FDA 510(k) record lists Mallinckrodt Critical Care as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNCUFFED REINFORCED TRACHEAL TUBE?
The FDA product code for UNCUFFED REINFORCED TRACHEAL TUBE is BTR.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Mallinckrodt Critical Care as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BTR)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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